Disease: Systolic Pressure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 9
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs1126930
PRKAG1 ; DDN-AS1
12 49005349 missense variant G/C snv 2.1E-02 2.1E-02 5
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27